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FITC標(biāo)記的(dí)過(guò)氧化物酶酰(xiān)基輔酶(méi)A氧(yǎng)化酶1抗體(tǐ)
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2017-5-3 瀏(liú)覽次數：1720
英文(wén)名稱Anti-ACOX1/FITC
中(zhōng)文名稱:FITC標(biāo)記(jì)的過氧化物酶(méi)酰基(jī)輔(fǔ)酶A氧化酶1抗體
別 名ACOX1; ACOX1_HUMAN; AOX antibody Palmitoyl CoA oxidase; Palmitoyl-CoA oxidase; Peroxisomal acyl coenzyme A oxidase 1; Peroxisomal acyl-coenzyme A oxidase 1; SCOX; Straight chain acyl CoA oxidase; Straight-chain acyl-CoA oxidase.
規(guī)格:100ul
說(shuō) 明 書100ul
研(yán)究(jiū)領(lǐng)域(yù)腫瘤 細胞(bāo)生(shēng)物 免(miǎn)疫學(xué) 轉錄(lù)調(tiáo)節因子
抗體來源(yuán)Rabbit
克(kè)隆類(lèi)型Polyclonal
交叉(chā)反應 Human, Mouse, Rat, Pig, Rabbit, Sheep,
產品(pǐn)應(yīng)用(yòng)IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分(fēn) 子 量74kDa
性 狀(zhuàng)Lyophilized or Liquid
濃(nóng) 度1mg/ml
免(miǎn) 疫(yì) 原KLH conjugated synthetic peptide derived from human ACOX1
亞 型IgG
純化方(fāng)法affinity purified by Protein A
儲 存 液(yè)0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件(jiàn)Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
產(chǎn)品介紹background:
Defects in ACOX1 are the cause of adrenoleukodystrophy pseudoneonatal (Pseudo-NALD); also known as peroxisomal acyl-CoA oxidase deficiency. Pseudo-NALD is a peroxisomal single-enzyme disorder. Clinical features include mental retardation, leukodystrophy, seizures, mild hepatomegaly, hearing deficit. Pseudo-NALD is characterized by increased plasma levels of very-long chain fatty cids, due to decreased or absent peroxisome acyl-CoA oxidase activity. Peroxisomes are intact and functioning.
中(zhōng)文名稱:FITC標(biāo)記(jì)的過氧化物酶(méi)酰基(jī)輔(fǔ)酶A氧化酶1抗體
別 名ACOX1; ACOX1_HUMAN; AOX antibody Palmitoyl CoA oxidase; Palmitoyl-CoA oxidase; Peroxisomal acyl coenzyme A oxidase 1; Peroxisomal acyl-coenzyme A oxidase 1; SCOX; Straight chain acyl CoA oxidase; Straight-chain acyl-CoA oxidase.
詳細(xì)介紹：
規(guī)格:100ul
說(shuō) 明 書100ul
研(yán)究(jiū)領(lǐng)域(yù)腫瘤 細胞(bāo)生(shēng)物 免(miǎn)疫學(xué) 轉錄(lù)調(tiáo)節因子
抗體來源(yuán)Rabbit
克(kè)隆類(lèi)型Polyclonal
交叉(chā)反應 Human, Mouse, Rat, Pig, Rabbit, Sheep,
產品(pǐn)應(yīng)用(yòng)IF=1:50-200
not yet tested in other applications.
optimal dilutions/concentrations should be determined by the end user.
分(fēn) 子 量74kDa
性 狀(zhuàng)Lyophilized or Liquid
濃(nóng) 度1mg/ml
免(miǎn) 疫(yì) 原KLH conjugated synthetic peptide derived from human ACOX1
亞 型IgG
純化方(fāng)法affinity purified by Protein A
儲 存 液(yè)0.01M TBS(pH7.4) with 1% BSA, 0.03% Proclin300 and 50% Glycerol.
保存條件(jiàn)Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.
相關資(zī)料：
產(chǎn)品介紹background:
Defects in ACOX1 are the cause of adrenoleukodystrophy pseudoneonatal (Pseudo-NALD); also known as peroxisomal acyl-CoA oxidase deficiency. Pseudo-NALD is a peroxisomal single-enzyme disorder. Clinical features include mental retardation, leukodystrophy, seizures, mild hepatomegaly, hearing deficit. Pseudo-NALD is characterized by increased plasma levels of very-long chain fatty cids, due to decreased or absent peroxisome acyl-CoA oxidase activity. Peroxisomes are intact and functioning.
